SNP Links for Nucleotide (Select 269847408) - SNP

Links from Nucleotide

Items: 1 to 20 of 25

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Select item 14616608131.

rs1461660813 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:33999990 (GRCh38)
6:33967767 (GRCh37)
Canonical SPDI:: NC_000006.12:33999989:A:T
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.0002/1 (ALFA)
T=0.0002/1 (Estonian)
HGVS:: NC_000006.12:g.33999990A>T, NC_000006.11:g.33967767A>T, NR_031681.1:n.62T>A

Select item 14192470892.

rs1419247089 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:34000011 (GRCh38)
6:33967788 (GRCh37)
Canonical SPDI:: NC_000006.12:34000010:G:C
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.34000011G>C, NC_000006.11:g.33967788G>C, NR_031681.1:n.41C>G

Select item 14066393963.

rs1406639396 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:34000036 (GRCh38)
6:33967813 (GRCh37)
Canonical SPDI:: NC_000006.12:34000035:C:A
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.34000036C>A, NC_000006.11:g.33967813C>A, NR_031681.1:n.16G>T

Select item 12702032114.

rs1270203211 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:33999997 (GRCh38)
6:33967774 (GRCh37)
Canonical SPDI:: NC_000006.12:33999996:T:C
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.33999997T>C, NC_000006.11:g.33967774T>C, NR_031681.1:n.55A>G

Select item 11574320395.

rs1157432039 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 6:34000009 (GRCh38)
6:33967786 (GRCh37)
Canonical SPDI:: NC_000006.12:34000008:C:G,NC_000006.12:34000008:C:T
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.34000009C>G, NC_000006.12:g.34000009C>T, NC_000006.11:g.33967786C>G, NC_000006.11:g.33967786C>T, NR_031681.1:n.43G>C, NR_031681.1:n.43G>A

Select item 9164370406.

rs916437040 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:34000003 (GRCh38)
6:33967780 (GRCh37)
Canonical SPDI:: NC_000006.12:34000002:T:C
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000006.12:g.34000003T>C, NC_000006.11:g.33967780T>C, NR_031681.1:n.49A>G

Select item 7748385857.

rs774838585 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:34000046 (GRCh38)
6:33967823 (GRCh37)
Canonical SPDI:: NC_000006.12:34000045:C:T
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.000008/1 (ExAC)
HGVS:: NC_000006.12:g.34000046C>T, NC_000006.11:g.33967823C>T, NR_031681.1:n.6G>A

Select item 7726916998.

rs772691699 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:34000033 (GRCh38)
6:33967810 (GRCh37)
Canonical SPDI:: NC_000006.12:34000032:A:G
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0./0 (TWINSUK)
G=0.0003/1 (ALSPAC)
HGVS:: NC_000006.12:g.34000033A>G, NC_000006.11:g.33967810A>G, NR_031681.1:n.19T>C

Select item 7693091579.

rs769309157 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:34000042 (GRCh38)
6:33967819 (GRCh37)
Canonical SPDI:: NC_000006.12:34000041:C:A
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000008/1 (ExAC)
HGVS:: NC_000006.12:g.34000042C>A, NC_000006.11:g.33967819C>A, NR_031681.1:n.10G>T

Select item 76657054110.

rs766570541 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33999975 (GRCh38)
6:33967752 (GRCh37)
Canonical SPDI:: NC_000006.12:33999974:C:T
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000024/6 (GnomAD_exomes)
T=0.000033/4 (ExAC)
HGVS:: NC_000006.12:g.33999975C>T, NC_000006.11:g.33967752C>T, NR_031681.1:n.77G>A

Select item 76166333211.

rs761663332 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 6:33999972 (GRCh38)
6:33967749 (GRCh37)
Canonical SPDI:: NC_000006.12:33999971:T:A
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000012/3 (GnomAD_exomes)
A=0.000017/2 (ExAC)
HGVS:: NC_000006.12:g.33999972T>A, NC_000006.11:g.33967749T>A, NR_031681.1:n.80A>T

Select item 76103436412.

rs761034364 [Homo sapiens]

Variant type:: DEL
Alleles:: GAC>- [Show Flanks]
Chromosome:: 6:34000018 (GRCh38)
6:33967795 (GRCh37)
Canonical SPDI:: NC_000006.12:34000017:GAC:
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000006.12:g.34000018_34000020del, NC_000006.11:g.33967795_33967797del, NR_031681.1:n.32_34del

Select item 75881178313.

rs758811783 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:34000022 (GRCh38)
6:33967799 (GRCh37)
Canonical SPDI:: NC_000006.12:34000021:G:A
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000111/1 (ALFA)
A=0.000008/1 (ExAC)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.34000022G>A, NC_000006.11:g.33967799G>A, NR_031681.1:n.30C>T

Select item 75501494914.

rs755014949 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:33999992 (GRCh38)
6:33967769 (GRCh37)
Canonical SPDI:: NC_000006.12:33999991:T:C
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000017/2 (ExAC)
HGVS:: NC_000006.12:g.33999992T>C, NC_000006.11:g.33967769T>C, NR_031681.1:n.60A>G

Select item 75406942515.

rs754069425 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33999981 (GRCh38)
6:33967758 (GRCh37)
Canonical SPDI:: NC_000006.12:33999980:C:T
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.000008/1 (ExAC)
HGVS:: NC_000006.12:g.33999981C>T, NC_000006.11:g.33967758C>T, NR_031681.1:n.71G>A

Select item 74737829716.

rs747378297 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 6:34000028 (GRCh38)
6:33967805 (GRCh37)
Canonical SPDI:: NC_000006.12:34000027:C:G,NC_000006.12:34000027:C:T
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000031/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/1 (ExAC)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.34000028C>G, NC_000006.12:g.34000028C>T, NC_000006.11:g.33967805C>G, NC_000006.11:g.33967805C>T, NR_031681.1:n.24G>C, NR_031681.1:n.24G>A

Select item 56162152117.

rs561621521 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:34000037 (GRCh38)
6:33967814 (GRCh37)
Canonical SPDI:: NC_000006.12:34000036:C:G
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000008/1 (ExAC)
G=0.000014/2 (GnomAD)
G=0.00002/5 (GnomAD_exomes)
G=0.000023/6 (TOPMED)
G=0.000106/2 (TOMMO)
G=0.000156/1 (1000Genomes)
HGVS:: NC_000006.12:g.34000037C>G, NC_000006.11:g.33967814C>G, NR_031681.1:n.15G>C

Select item 55792812118.

rs557928121 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:34000019 (GRCh38)
6:33967796 (GRCh37)
Canonical SPDI:: NC_000006.12:34000018:A:T
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000012/3 (GnomAD_exomes)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000006.12:g.34000019A>T, NC_000006.11:g.33967796A>T, NR_031681.1:n.33T>A

Select item 37718820319.

rs377188203 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:34000023 (GRCh38)
6:33967800 (GRCh37)
Canonical SPDI:: NC_000006.12:34000022:C:T
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000113/5 (ALFA)
T=0.000041/10 (GnomAD_exomes)
T=0.000058/7 (ExAC)
T=0.000242/34 (GnomAD)
T=0.000242/64 (TOPMED)
T=0.000312/2 (1000Genomes)
T=0.000485/5 (GoESP)
HGVS:: NC_000006.12:g.34000023C>T, NC_000006.11:g.33967800C>T, NR_031681.1:n.29G>A

Select item 37472838520.

rs374728385 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 6:34000032 (GRCh38)
6:33967809 (GRCh37)
Canonical SPDI:: NC_000006.12:34000031:C:A,NC_000006.12:34000031:C:G
Gene:: MIR1275 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000056/2 (ALFA)
A=0.000025/3 (ExAC)
A=0.000072/19 (TOPMED)
A=0.000097/1 (GoESP)
HGVS:: NC_000006.12:g.34000032C>A, NC_000006.12:g.34000032C>G, NC_000006.11:g.33967809C>A, NC_000006.11:g.33967809C>G, NR_031681.1:n.20G>T, NR_031681.1:n.20G>C

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